The Gorlin-Goltz syndrome or (the nevoid basal cell carcinoma syndrome) is a rare autosomal dominant syndrome with multiple organ involvements. The common manifestations include multiple odontogenic keratocysts in the jaws, multiple basal cell nevi on the skin with an early age onset, palmar pits, bifid or splayed ribs, high arched palate, euryopia, areas of hyper-pigmentation in the upper eyelid of left eye and dorsal surface of hands, calcified diaphragma sellae, and calcifications of the falx cerebri. In this case report, we report the only case of Gorlin-Goltz syndrome in the Jammu-Kashmir region in a young 20-year-old female patient.

The ischiogluteal bursitis which is a rare disorder is irregularly found between the gluteus maximus and ischial tuberosity. A 41-year-old female with bilateral calcifying ischiogluteal bursitis and her right shoulder tendinopathy were presented. She had no related past medical history nor trauma to the buttock. Ischiogluteal bursitis Aspiration showed calcareous deposits; local injection of corticosteroid helped the patient to get free of symptoms. Calcified ischiogluteal bursitis is a rare condition but simply diagnosed on x-ray. Local steroid injection could provide symptom relief.